Health Sciences Research Centre, Faculty of Health Sciences of the University of Beira Interior (CICS-UBI), Av. Infante D. Henrique, 6201-556, Covilhã, Portugal.
Pharmaco-Toxicology Laboratory-UBIMedical, University of Beira Interior, Estrada Municipal 506, 6200-284, Covilhã, Portugal.
Anal Bioanal Chem. 2020 Nov;412(28):7963-7976. doi: 10.1007/s00216-020-02929-6. Epub 2020 Sep 22.
Cocaine is still one of the most commonly used illicit substances worldwide, with an estimated 4 million users in Europe in the last year. Hair samples have been widely used for the determination of episodic or repeated consumption of this substance, but the use of miniaturized techniques for hair sample clean-up has been challenging due to the sample complexity. Despite hair's complex matrix, MEPS provides a method that is fast, reduces the volume of extraction solvents used, and offers low-cost options (since extraction beds may be reused several times). Microextraction by packed sorbent using a mixed-mode sorbent was optimized for hair sample clean-up in order to determine cocaine, benzoylecgonine, ecgonine methyl ester, norcocaine, cocaethylene and anhydroecgonine methyl ester by gas chromatography coupled to tandem mass spectrometry. The method was fully validated according to internationally accepted criteria, presenting good linearity between the limits of quantification (0.01-0.15) and 5 ng/mg. Precision and accuracy resulted in coefficients of variation typically lower than 15%, with mean relative errors within ±15% for all compounds, except for the limit of quantification (±20%). The present work describes the first application of microextraction by packed sorbent for the concentration of cocaine and metabolites extracted from hair samples. Graphical abstract.
可卡因仍然是全球最常用的非法物质之一,据估计,去年欧洲有 400 万使用者。头发样本已广泛用于确定该物质的偶发性或重复性消费,但由于样本复杂性,对头发样本进行微型化处理的技术应用一直具有挑战性。尽管头发基质复杂,但 MEPS 提供了一种快速、减少提取溶剂用量且具有低成本选择的方法(因为提取床可重复使用多次)。使用混合模式吸附剂的填充吸附剂微萃取已针对头发样本净化进行了优化,以便通过气相色谱-串联质谱法测定可卡因、苯甲酰古柯碱、ecgonine 甲酯、去甲可卡因、可乐定和脱水 ecgonine 甲酯。该方法根据国际公认的标准进行了全面验证,在定量下限(0.01-0.15)和 5 ng/mg 之间呈现出良好的线性关系。精密度和准确度导致变异系数通常低于 15%,除了定量下限(±20%)之外,所有化合物的平均相对误差均在±15%以内。本工作描述了微萃取填充吸附剂首次应用于从头发样本中提取可卡因和代谢物的浓缩。